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Oded Abramsky

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Aging and Disease|June 24, 2024
Ovariectomy and High Fat-Sugar-Salt Diet Induced Alzheimer's Disease/Vascular Dementia Features in MiceSahar Sweetat, Moti Ben Shabat, Paschalis Theotokis, et al.
Brain : a Journal of Neurology|November 19, 2004
A novel autosomal recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12Alexander Lossos, Lekbir Baala, Dov Soffer, et al.
Experimental Neurology|May 21, 2008
A novel transgenic mouse expressing double mutant tau driven by its natural promoter exhibits tauopathy characteristicsHanna Rosenmann, Nikolaos Grigoriadis, Hila Eldar-Levy, et al.
Archives of Neurology|October 13, 2010
Safety and immunological effects of mesenchymal stem cell transplantation in patients with multiple sclerosis and amyotrophic lateral sclerosisDimitrios Karussis, Clementine Karageorgiou, Adi Vaknin-Dembinsky, et al.
Brain : a Journal of Neurology|November 30, 2020
Beneficial effects of autologous mesenchymal stem cell transplantation in active progressive multiple sclerosisPanayiota Petrou, Ibrahim Kassis, Netta Levin, et al.
Archives of Neurology|May 10, 2006
Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneityAlexander Lossos, Giovanni Stevanin, Vardiella Meiner, et al.
Journal of Neurology|July 22, 2015
Frequent misdiagnosis of adult polyglucosan body diseaseMark A Hellmann, Or Kakhlon, Ezekiel H Landau, et al.
Archives of Neurology|April 13, 2005
Early clinical heterogeneity in choreoacanthocytosisAlexander Lossos, Carol Dobson-Stone, Anthony P Monaco, et al.
Plos One|December 29, 2012
T cell vaccination benefits relapsing progressive multiple sclerosis patients: a randomized, double-blind clinical trialDimitrios Karussis, Hagai Shor, Julia Yachnin, et al.
JAMA Neurology|May 7, 2014
Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegiaAlexander Lossos, Omri Teltsh, Tsipi Milman, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
Aging and Disease|June 24, 2024
Ovariectomy and High Fat-Sugar-Salt Diet Induced Alzheimer's Disease/Vascular Dementia Features in MiceSahar Sweetat, Moti Ben Shabat, Paschalis Theotokis, et al.
Brain : a Journal of Neurology|November 19, 2004
A novel autosomal recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12Alexander Lossos, Lekbir Baala, Dov Soffer, et al.
Experimental Neurology|May 21, 2008
A novel transgenic mouse expressing double mutant tau driven by its natural promoter exhibits tauopathy characteristicsHanna Rosenmann, Nikolaos Grigoriadis, Hila Eldar-Levy, et al.
Archives of Neurology|October 13, 2010
Safety and immunological effects of mesenchymal stem cell transplantation in patients with multiple sclerosis and amyotrophic lateral sclerosisDimitrios Karussis, Clementine Karageorgiou, Adi Vaknin-Dembinsky, et al.
Brain : a Journal of Neurology|November 30, 2020
Beneficial effects of autologous mesenchymal stem cell transplantation in active progressive multiple sclerosisPanayiota Petrou, Ibrahim Kassis, Netta Levin, et al.
Archives of Neurology|May 10, 2006
Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneityAlexander Lossos, Giovanni Stevanin, Vardiella Meiner, et al.
Journal of Neurology|July 22, 2015
Frequent misdiagnosis of adult polyglucosan body diseaseMark A Hellmann, Or Kakhlon, Ezekiel H Landau, et al.
Archives of Neurology|April 13, 2005
Early clinical heterogeneity in choreoacanthocytosisAlexander Lossos, Carol Dobson-Stone, Anthony P Monaco, et al.
Plos One|December 29, 2012
T cell vaccination benefits relapsing progressive multiple sclerosis patients: a randomized, double-blind clinical trialDimitrios Karussis, Hagai Shor, Julia Yachnin, et al.
JAMA Neurology|May 7, 2014
Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegiaAlexander Lossos, Omri Teltsh, Tsipi Milman, et al.
Pageof 7